- In
carbohydrate chemistry, a pair of
anomers (from Gr**** ἄνω 'up, above', and μέρος 'part') is a pair of near-identical
stereoisomers or diastereomers...
-
material in a
solution due to a
change in
proportion of the two
constituent anomers (i.e. the
interconversion of
their respective stereocenters)
until equilibrium...
- alpha-Arbutin, or α-arbutin, is a
glycosylated hydroquinone, and an
anomer of the
naturally occurring arbutin. α-Arbutin is used in the
cosmetic and pharmaceutical...
- at the
anomeric carbon are
called anomers. The
anomers of D-glucopyranose are diastereomers, with the beta
anomer having a
hydroxyl (−OH)
group pointing...
- 2',6,6'-Tetrasubstituted
biphenyls can fit into this
latter category.
Anomerism is an
identity for
single bonded ring
structures where "cis" or "Z" and...
- R* descriptor. To
designate two
anomers the
relative stereodescriptors alpha (α) and beta (β) are used. In the α
anomer the
anomeric carbon atom and the...
-
which is not
involved in a
glycosidic bond,
could be
either an α- or β-
anomer depending on the bond
direction of the
attached hydroxyl group relative...
- the ring. The
resulting possible pair of
stereoisomers is
called anomers. In the α
anomer, the -OH
substituent on the
anomeric carbon rests on the opposite...
- last
stereogenic center the
sugar is the α-
anomer when they are
opposite the
sugar is the β-
anomer.
Anomers can be
interconverted through a
process known...
- α-D-glucopyranosyl residue,
which was
later redetermined to be the β-D-glucopyranosyl
anomer.
Carminic acid is
commonly harvested from an
American species scaled insects...
